Enhanced Photocatalytic Reduction of Methyl Viologen by Self

Masahiro Suzuki, Chad C. Waraksa, Thomas E. Mallouk*, Hiroko Nakayama, and Kenji Hanabusa. Department of Chemistry, The Pennsylvania State University,...
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J. Phys. Chem. B 2002, 106, 4227-4231

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Enhanced Photocatalytic Reduction of Methyl Viologen by Self-Assembling Ruthenium(II)Poly(Pyridyl) Complexes with L-Lysine Containing Side Chains Masahiro Suzuki, Chad C. Waraksa, Thomas E. Mallouk,* Hiroko Nakayama,† and Kenji Hanabusa† Department of Chemistry, The PennsylVania State UniVersity, UniVersity Park, PennsylVania 16802 ReceiVed: NoVember 2, 2001; In Final Form: January 24, 2002

New tris(2,2′-bipyridine)-type ruthenium(II) complexes with L-lysine-containing side chains form gels by hierarchical assembly of hydrogen bonded fibers in some organic solvents. These Ru(II) complex aggregates are more efficient photosensitizers for reduction of methyl viologen than Ru(bpy)32+ in the presence of triethanolamine, a sacrificial electron donor. The increased rate of reduced viologen formation arises from an increased charge separation lifetime and an increased rate of reduction of Ru(III) to Ru(II) by triethanolamine.

Introduction Self-assembly is one of the most useful tools available to chemists for organizing complex photoredox systems for vectorial electron transfer. In the broadest definition, selfassembly refers to a process by which a structurally well-defined supramolecular aggregate forms spontaneously from its component molecules. Well-known examples include monolayer assembly, membrane formation, molecular recognition (i.e., substrate binding to proteins, DNA/protein interactions, antibody/ antigen interactions), metal ion coordination, and fiber and network assemblies.1-3 These structures are held together by relatively weak intermolecular forces which include hydrogen bonding, π-stacking, van der Waals interactions, hydrophobic/ hydrophilic interactions, ionic forces, and relatively labile metal-ligand coordination interactions. Often, these materials are characterized by hierarchical structures, i.e., by organization on more than one length scale. Many low molecular weight compounds that form a hierarchical network of superstructures in organic fluids have now been synthesized3-5 and have been applied to the fabrication of templated materials,6,7 sensors,8 and assemblies with molecular recognition and other useful properties.9,10 Recently, we have reported the supramolecular structure of L-lysine derivatives that form nanometer-scale fibers in various organic fluids.11 These compounds create a hierarchical network by entangling of fibers, and they can gel many organic solvents. More recently, an L-lysine viologen derivative, which forms fibrous aggregates in some aromatic solvents, has been synthesized, and its photosensitized charge separation reaction has been investigated using Ru(bpy)32+ as a photosensitizer.12 The initial rate of viologen radical formation for this self-assembling system is higher than that for methyl viologen (MV2+) in the analogous homogeneous system. Here, we describe the synthesis of new ruthenium(II)poly(pyridyl) complexes with L-lysine containing side chains. These photosensitizers form nanometer scale fibrous assemblies, and show enhanced quantum yields for MV2+ photoreduction in methanol-toluene (1:1 v/v), in the presence * To whom correspondence should be addressed. † Graduate School of Science and Technology, Shinshu University, Ueda, Nagano 386-8567, Japan.

of the sacrificial donor triethanolamine (TEOA), relative to Ru(bpy)32+ in the same system. Experimental Section Materials. N--Lauroyl-L-lysine was supplied from Ajinomoto Co., Inc. All other starting materials were purchased from chemical suppliers and used without further purification. 4,4′Dimethyl-2,2′-bipyridine,11 4,4′-dicarboxy-2,2′-bipyridine,11 4,4′bis(chlorocarbony)-2,2′-bipyridine,11 and N--lauroyl-L-lysine ethyl ester (C2AmiNH2)9 were synthesized according to literature procedures. Synthesis of 2,2′-Bipyridine Ligand with N--Lauroyl-Llysine Ethyl Esters [(C2Ami)2bpy]. C2AmiNH2 was dissolved in a dry THF solution containing NEt3, and a dry THF solution of 4,4′-bis(chlorocarbonyl)-2,2′-bipyridine was slowly added in an ice-bath with stirring. The resulting solution was stirred at room temperature for 24 h. The white precipitate was filtered and washed with THF. The mixture of the filtrate and washings was evaporated to dryness. The crude product was dissolved in hot methanol, and the hot solution was quickly filtered. The pure white product was obtained by cooling in a refrigerator for 6 h. Elemental Anal. Calcd. for C52H84N6O8: C, 67.78; H, 9.21; N, 9.12. Found: C, 67.89; H, 9.22; N, 9.29. Yield 91%. Synthesis of Ruthenium(II) Complexes. Tris[(C2Ami2)bpy]ruthenium(II) chloride hexahydrate Ru[(C2Ami2)bpy]3Cl2‚6H2O (Ru1). RuCl3‚3H2O and [(C2Ami2)bpy] were refluxed in ethanol for 5 d. The hot solution was filtered and evaporated to dryness. The crude solid was dissolved in toluene and filtered. The filtrate was evaporated to dryness. Elemental Anal. Calcd. for C156H264N18O24Cl2Ru: C, 61.55; H, 8.76; N, 8.27. Found: C, 61.88; H, 8.92; N, 8.12. Yield 88%. Ru[(C2Ami)2bpy][bpy]2Cl2‚6H2O (Ru2)‚Ru(bpy)2Cl2‚2H2O and (C2Ami)2bpy were refluxed in 80% ethanol for 2 d under an argon atmosphere. The solution was evaporated to dryness. The crude solid was dissolved in a cold acetone, and the insoluble compound was filtered off. The Ru[C2Ami)2bpy][bpy]2Cl2‚6H2O was obtained by evaporation of the filtrate to dryness. Elemental Anal. Calcd. for C72H112N10O14Cl2Ru: C, 57.12; H, 7.47; N, 9.25. Found: C, 57.34; H, 7.62; N, 9.33. Yield 92%. Measurements. Elemental analyses were performed with a Perkin-Elmer series II CHNS/O analyzer 2400. FTIR spectra

10.1021/jp014050h CCC: $22.00 © 2002 American Chemical Society Published on Web 03/30/2002

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SCHEME 1

were recorded on a JASCO FS-420 spectrometer. UV-Vis absorption spectra were acquired on a Hewlett-Packard HP8452A diode array spectrometer or a JASCO V-570 UV/VIS/NIR spectrophotometer. Luminescence spectra were measured using a JASCO FP-750 spectrofluorimeter. Gelation Test. In a typical gelation test, a weighed amount of Ru1 or Ru2 and 1 mL of solvent were combined in a glass test tube (1 cm diameter), which was sealed and then heated until complete dissolution was observed. The solution was allowed to cool to room temperature. Gelation was judged to have occurred when a homogeneous solution was obtained which did not flow when the test tube was tilted or inverted. Transmssion Electron Microscopy (TEM). TEM images were obtained with a JEOL JEM-2010 electron microscope at 100 kV. Samples were prepared as follows: the compounds were dissolved in toluene or toluene-methanol and a drop of the solution was put on a collodion and carbon-coated 400 mesh copper grid. The grids were stored in a desiccator for 6 h, and then stored under reduced pressure overnight. Steady-State Photolysis. Steady-state photolysis studies were conducted using the same apparatus described previously.14 The reactions were carried out in methanol-toluene containing 1.1 × 10-5 M Ru complex and 1.0 × 10-3 M methyl viologen under an argon atmosphere at ambient temperature (22-24°). A spectroscopic cell (0.2 cm path length) was irradiated using a 300 W Xe lamp (ORIEL 500 W Xe and Hg/Xe arc lamp supply model 68811, ORIEL Co.) equipped with a UV cutoff filter (λ > 440 nm). Prior to the photolysis experiments, oxygen was expelled by bubbling argon gas into the sample solution for 15 min. The formation of the viologen radical calculated from the absorbance of the solution at 606 nm, corresponding to the maximum wavelength of the viologen radical (605 ) 13400 mol-1 dm3 cm-1), and was monitored as a function of irradiation time. The initial rates of the viologen radical formation were calculated from the initial slope of a plot of the concentration of the viologen radical versus irradiation time. In all systems, the experimental errors were within ( 0.5%.

Nanosecond Flash Photolysis/Transient Diffuse Reflectance. Transient absorbance and emission measurements were carried out as described in detail elsewhere.15 A 150 W Xe arc lamp was focused through a shutter window and 340 nm long pass filter onto the face of the cuvette at 45°. Approximately normal to the Xe light source, a 532 nm, 15 ns pulsed laser (Spectra Physics GCR-13 Nd:YAG, ca. 200 mJ/pulse) illuminated the same area of the cuvette. Results and Discussion Amphiphilic L-lysine derivatives are known for their gelforming properties in organic solvents. The 2,2′-bipyridine ligand containing an L-lysine derivative at the 4,4′-positions [(C2Ami)2bpy] and ruthenium(II) complexes (Ru1 and Ru2) were prepared according to Scheme 1. The synthesis of these Ru complexes follows easily from the (C2Ami)2bpy ligand, and in principle can be adapted to make gel-forming derivatives of a variety of transition metal polypyridyl complexes. Ru2, which contains a single (C2Ami)2bpy ligand, has the ability to gel some aromatic solvents such as benzene, chlorobenzene, nitrobenzene, and chlorobenzene. In the same media, Ru1, which contains three (C2Ami)2bpy ligands, forms isotropic solutions. The minimum concentration for gelation of Ru2 is 2 mg/mL in benzene and 4 mg/mL in toluene. Figure 1 shows TEM images of Ru1 and Ru2 prepared from toluene. Although both Ru1 and Ru2 form fiber structures, Ru2 creates the network by entanglement of fine fibers. This hierarchical network structure is responsible for the gelation of Ru2. In contrast, Ru1 forms a helical structure,16 but not a network gel. FTIR spectra were helpful in understanding the self-assembly of Ru1 and Ru2. Spectra in chloroform, in which no selfassembly occurs, show absorption bands at 3440 and 1665 cm-1, which are characteristic N-H and CdO stretching frequencies for non-hydrogen bonded amide groups. In contrast, spectra in toluene are very similar to those obtained for the complexes in the solid state. Both contain a band at 3320 cm-1, which is

Photocatalytic Reduction of Methyl Viologen

J. Phys. Chem. B, Vol. 106, No. 16, 2002 4229 TABLE 2: Kinetic Parameters Obtained from Steady-state and Laser Flash Photolysis ratea kq/108 [µM s-1] [M-1s-1] Ru1 Ru2 Ru(bpy)32+

24.1 9.8 5.1

1.54 1.83 5.52

φqb 0.18 0.15 0.32

kb/1010 c ks/107 d k0/104 e [M-1s-1] [M-1s-1] [s-1] 0.69 1.16 4.96

4.35 2.82 1.67

2.2 2.4 12.0

a Initial rate of MV+• formation at [Ru(II)] ) 1.1 × 10-5 M, [MV2+] ) 1.0 × 10-3 M, and [TEOA] ) 0.1 M. b Quantum yield for electrontransfer quenching of the MLCT excited state, from eq 4, using τ () 1/kr) values from Table 1. c Rate constants for back electron transfer obtained from MV+• decay curves at [Ru(II)] ) 1.1 × 10-5 M and [MV2+] ) 3.0 × 10-3 M. d Rate constant for reduction of Ru(III) by TEOA, from bleaching recovery of the Ru(II) transient absorbance. e Average k value, as defined in eq 12, for each sensitizer obtained by 0 fitting steady-state photolysis data at [Ru(II)] ) 1.1 × 10-5 M, [MV2+] ) 1.0 × 10-3 M.

Figure 1. TEM images of Ru1 (left) and Ru2 (right) prepared from toluene. Scale bars are 200 and 500 nm, respectively.

Scheme 2a

a (i) dry THF/dry NEt ; (ii) RuCL 3H O/EtOH; (iii) Ru(bpy) Cl 3 3 2 2 2 2H2O/80% EtOH.

Figure 2. UV-vis absorption and luminescence spectra of Ru1 (solid line) and Ru2 (dotted line) in methanol-toluene (1:1, v/v). [Ru1] ) 4.1 × 10-5 M and [Ru2] ) 3.8 × 10-5 M.

TABLE 1: Photochemical and Photophysical Properties of a Series of Ru(II) Complexes compd

λmax,absa ()

λmax,emb

τ/µsc

Ru1 Ru2 Ru(bpy)32+

466 (22 000)d 468 (17 000)d 452 (14 500)d

655 622 611

1.42 0.98 0.85

a Absorption maxima (nm). b Luminescence maxima (nm). c Excitedstate lifetimes at luminescence maxima obtained by laser flash photolysis.

assigned to the N-H vibration of hydrogen bonded amide groups. This indicates that hydrogen bonding contributes to the driving force for self-assembly. For Ru2, fine nanofibers are entangled in a complex way, probably through van der Waals interactions between terminal alkyl groups, and the network structure that leads to gelation is created. By analogy to the well studied sensitizer Ru(bpy)32+, the visible electronic transitions of Ru1 and Ru2 can be attributed to metal-to-ligand charge-transfer (MLCT), and emission occurs from the predominantly triplet MLCT excited state. Figure 2 shows absorption and emission spectra of Ru1 and Ru2 under conditions where both complexes exist in the solution state. Spectroscopic data for Ru1 and Ru2 are compared in Table 1 to those of Ru(bpy)32+ in the same solvent system. The MLCT bands of Ru1 and Ru2 are red-shifted relative to Ru(bpy)32+ and the extinction coefficients are larger; in particular, that of Ru1 is almost double that of Ru(bpy)32+. Both Ru1 and Ru2 have red-shifted luminescence and longer MLCT excited-state lifetimes than Ru(bpy)32+. These differences are significantly larger for Ru1 than for Ru2. Because Ru1 has many hydrogen bonding sites, we postulate that it is more strongly interacting

than Ru2 in the self-assembling fibers. The thermal motion between Ru(II) and ligands is therefore more restricted in the case of Ru1, and this leads to a higher luminescence intensity and longer MLCT excited-state lifetime. Under an argon atmosphere, methyl viologen radical (MV+•) was formed by visible light irradiation (λ > 440 nm) of methanol-toluene solutions containing Ru(II) photosensitzers, methyl viologen (MV2+), and triethanolamine (TEOA). The concentrations of sensitizers (1.1 × 10-5 M in methanol-toluene) was kept well below the gel transition in these experiments. Interestingly, with the self-assembling Ru(II) photosensitizers, the initial rate of MV+• formation was higher; in particular, the initial rate with Ru1 was about five times as high as that with Ru(bpy)32+ (Table 2). Because this enhancement in photoreduction yield is larger than can be accounted for by the longer MLCT lifetime of Ru1, we conducted a kinetic analysis to determine whether the increased rate was a consequence of supramolecular organization. To consider the reaction mechanism in more detail, the rate constants for the elementary reactions were measured using laser flash photolysis. In these systems, the charge separation reaction proceeds according to Scheme 2 and its initial rate depends on the quenching (forward) reaction, the rate of back electron transfer from MV+• to Ru(III), and the rate of reduction of Ru(III) to Ru(II) by TEOA. Dynamic Stern-Volmer plots for quenching of the MLCT excited state by methyl viologen, Figure 3, were linear for Ru1, Ru2, and Ru(bpy)32+. As shown in Table 2, the rate constant for quenching of the excited state (kq) was highest for Ru(bpy)32+. Interestingly, Ru1, which has the highest rate of MV+• formation under steady-state photolysis conditions, has the smallest value of kq. Table 2 gives rate constants derived from transient absorbance changes at 605 nm, where MV+• absorbs strongly, following laser excitation of Ru1, Ru2, and Ru(bpy)32+ containing methanol-toluene solutions. The MV+• decay at 605 nm obeys second-order kinetics and the second-order rate constants (kb) are in the order of Ru1 < Ru2 < Ru(bpy)32+: that is, the lifetime of MV+• in the self-assembling Ru(II) complex systems is substantially longer than that in the Ru(bpy)32+ system.

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φce )

kce kce + kcr

(7)

Once formed by reaction 5, Ru (III) can be reduced to Ru (II) by reaction with TEOA or MV+• according to eqs 8 or 9, respectively. Again, from the branching of these two ks

[RuL3]3+ + TEOA 98 [RuL3]2+ + decomposition products (8) kb

[RuL3]3+ + MV+• 98 [RuL3]2+ + MV2+ Figure 3. Stern-Volmer plots for luminescence quenching of Ru1 2+ in methanol-toluene. (J), Ru2 (B), and Ru(bpy)2+ 3 (H) by MV

Moreover, the second-order rate constant for reduction of Ru(III) to Ru(II) by TEOA (ks), determined by measuring the Ru(II) bleaching recovery rate at different TEOA concentrations, are in the order of Ru1 > Ru2 > Ru(bpy)32+. These results indicate that the more effective charge separation for the self-assembling photosensitizers is caused by a slow back reaction with MV+• and fast scavenging of Ru(III), relative to the Ru(bpy)32+ system. The TEOA molecules, which contain functional hydrogen bond donor and acceptor groups, are most likely concentrated around the Ru(II) complex-core by hydrogen bonding. The slower rate constants for quenching of the excited state, as well as the slower back reactions between MV+• and Ru(III), are tentatively attributed to Coulombic repulsion between the self-assembling fibers and the cationic viologen ions. Similar slowing of forward and back electron-transfer rates has been observed with polyelectrolyte sensitizers and acceptors in aqueous systems.17 The rate constants measured by transient spectroscopy can be related quantitatively to the steady-state photolysis yields by considering the reaction mechanism in more detail. Steadystate irradiation produces the MLCT excited state at a constant rate, khν, according to reaction 1. The excited state decays by a combination of radiative and nonradiative pathways, one of which is quenching by MV2+ (2). The remainder can be grouped together into the first-order decay reaction 3, which is characterized by the rate constant kr khν

[RuL3]2+ 98 [RuL3]2+* kq

[RuL3]2+* + MV2+ 98 {[RuL3]3+ - - - MV+•} kr

[RuL3]2+* 98 [RuL3]2+

(1) (2) (3)

The quenching yield φq may be calculated from kq and kr according to (4). Once formed, the caged {[RuL3]3+ - - - MV+•}complex can separate by reaction 5 or undergo back electron

φq )

kq[MV2+] kq[MV2+] + kr

(4)

transfer 6 to regenerate the reactants. The cage escape kce

{[RuL3]3+ - - - MV+•} 98 [RuL3]3+ + MV+• kcr

{[RuL3]3+ - - - MV+•} 98 [RuL3]2+ + MV2+ yield φce is derived from kce and kcr according to 7

(5) (6)

(9)

kinetic pathways, the quantum yield for reduction of Ru(III) by TEOA may be calculated eq 10

φs )

ks[TEOA] ks[TEOA] + kb[MV+•]

(10)

By combining these quantum yields with the generation rate khν, we obtain a differential eq 11 that describes the rate of formation of MV+•

ks[TEOA] d[MV+•] ) khνφqφceφs ) k0 dt ks[TEOA] + kb[MV+•]

(11)

In which k0 is defined as

k0 ≡ khνφqφce

(12)

Solving this equation gives the integrated rate law 13

[MV+•] )

{

k0ks[TEOA] 1 - + kb k0

[( )

2kbt 1 2 + k0 k0ks[TEOA]

]} 1/2

(13)

which predicts a linear growth in MV+• concentration at early times in the reaction, followed by an approximately t1/2 growth at later times. Figure 4 shows steady-state photolysis data, along with the behavior expected from eq 13. Individual k0 values were obtained by one-parameter fitting of photolysis data acquired over a range (0.1 to 1.0 M) of TEOA concentrations. In each case the fit was constrained by the ks/kb ratio (Table 2) measured by transient spectroscopy. The lines shown in Figure 4, which use the average of the k0 values obtained for each sensitizer (Table 2), fit the data only approximately. This is especially true at longer times where background processes (such as reaction of MV+• with water and oxygen) cause some flattening of the expected t1/2 behavior. A number of factors could contribute to the observed systematic departure from the simple (homogeneous) kinetic model proposed above. Although the MLCT decays are singleexponential for Ru1 and Ru2 (implying that the microenvironment is similar for all sensitizer molecules), the distribution of MV2+ and TEOA in the nanofibers is not necessarily homogeneous. Diffusion of molecules in these organized media is most likely not a stochastic process. Other factors, such as background oxidation or decomposition of viologen radicals, could also contribute to flattening of the photolysis curves. Nevertheless, the general shape of all the curves, including those not shown, is roughly that expected from the kinetic model, and so conclusions can be drawn from the major trends. We note that the ordering of k0 values derived for Ru1, Ru2, and Ru(bpy)32+ follows the trend in φq, as expected from eq 12. By

Photocatalytic Reduction of Methyl Viologen

J. Phys. Chem. B, Vol. 106, No. 16, 2002 4231 References and Notes

Figure 4. Steady state photolysis plot for Ru1, Ru2, and -5 M, [MV2+] ) 1.0 × 10-3 M, and Ru(bpy)2+ 3 at [Ru(II)] ) 1.1 × 10 [TEOA] ) 0.1 M. Solid lines show the behavior predicted from eq 13, using ks and kb values from Table 2. The k0 values used to plot the lines are averages obtained from single parameter fits to eq 13, obtained over a range of TEOA concentrations.

comparing k0 values, we can also conclude that the cage escape yields, φce, are significantly lower for Ru1 and Ru2 than they are for Ru(bpy)32+. Conclusions We have found that Ru(II) complex photosensitizers containing L-lysine side chains form fibrous supramolecular structures. Despite their lower quenching rates and cage escape yields, the photolysis reaction is more efficient with Ru1 and Ru2 than it is with Ru(bpy)32+. The improvement derives from the much slower back electron-transfer rates, kb, and the enhanced rates of the donor reaction, ks, for the supramolecular sensitizers. These effects are most pronounced for Ru1, which contains six L-leucine containing side chains, than they are for Ru2, which contains only two such side chains. Laser flash photolysis measurements confirm that the lifetime of MV+• in these systems is long and that the reduction of the Ru(III) to Ru(II) is fast compared to the simple Ru(bpy)32+ system. These results are encouraging for the design of other donor-sensitizer-acceptor systems, because they demonstrate that hydrogen bonding and Coulombic effects in supramolecular aggregates of sensitizers can be used effectively to enhance photoproduct yields. Acknowledgment. This work was supported by the Division of Chemical Sciences, Office of Basic Energy Sciences, Department of Energy, under Contract No. DE-FG02-93ER14374 and Grant-in-Aid for COE research (10CE2003) from the Ministry of Education, Culture, Science, Sports, and Technology of Japan.

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